Polylactam composition containing hexaorgano distannane

ABSTRACT

Hexaorgano distannanes of the general formula R 3  Sn--SnR 3  significantly reduce or eliminate the discoloration which occurs when mixtures containing an alkali metal salt of a lactam are stored under an inert atmosphere for extended periods of time at temperatures between ambient and 100° C. R in the foregoing formula represents a monovalent hydrocarbon radical containing between 1 and 20 carbon atoms.

This is a divisional of application Ser. No. 430,690 filed Jan. 4, 1974, now U.S. Pat. No. 3,954,738.

BACKGROUND

This invention relates to the stabilization of salts derived from a lactam and an alkali metal.

Lactams of the general formula ##STR1## are employed as starting materials for the preparation of high molecular weight polyamides. The homopolymer of ε-caprolactam is often referred to as "nylon 6". These lactam polymers exhibit excellent tensile properties and can be formed into a variety of useful products including textile denier fibers, films, castings and molded objects. Pure, dry lactams, particularly ε-caprolactam, do not polymerize appreciably even at elevated temperatures; however the polymerization can be activated using any one of a large number of materials as catalysts. Alkali metal salt of lactams are particularly effective catalysts, and are discussed by W. E. Hanford and R. M. Joyce [Journal of Polymer Science, Volume 3, No. 2, pages 167-172 (1948)]. The polymerization proceeds rapidly at temperatures between 200° and 280° C. and is conveniently carried out by adding the desired amount of alkali metal to the lactam to effect, first, salt formation, followed by a polymerization which is catalyzed by the salt. A major shortcoming of the alkali metal salts of lactams is that they discolor relatively rapidly even under inert atmospheres, particularly at the elevated temperatures employed to liquefy and polymerize lactams. The color imparted to the resultant polymer renders it unacceptable for many ends uses, particularly as textile fiber and film.

It is therefore an object of the present invention to eliminate or at least significantly reduce the discoloration which occurs in compositions containing an alkali metal salt of a lactam.

A second objective of this invention is to stabilize polymerizable mixtures containing a lactam and an alkali metal salt of said lactam without adversely affecting the activity of the alkali metal salt as a latent polymerization catalyst.

It has now been found that these objectives can be attained when a hexaorgano distannane is present in combination with an alkali metal lactam salt.

SUMMARY OF THE INVENTION

The present invention provides stabilized compositions containing an alkali metal salt of a lactam, wherein said salt exhibits the general formula ##STR2## and a hexaorgano distannane of the general formula R₃ ² Sn--SnR₃ ³, in an amount between 0.5 and about 100%, based on the weight of said salt, wherein R¹ represents an alkylene radical containing between 2 and 6 carbon atoms, inclusive, and M represents an alkali metal selected from the group consisting of lithium, sodium and potassium. R² and R³ are individually selected from the group consisting of alkyl radicals containing between 1 and 20 carbon atoms, cycloalkyl, aralkyl, aryl and alkaryl radicals.

This invention further provides improved compositions suitable for use in preparing polyamides or polyesteramides by the catalyzed homopolymerization or copolymerization of lactams. These compositions contain one or more lactams and a catalytic amount of an alkali metal salt of a lactam, wherein the improvement resides in the presence of between 0.5 and 100%, based on the weight of said salt, of a hexaorgano distannane.

DETAILED DESCRIPTION OF THE INVENTION

The alkali metal lactam salts that can be stabilized against discoloration using the present hexaorgano distannanes are derived from the reaction of the corresponding alkali metals, which include lithium, sodium and potassium, with lactams i.e. cyclic amides of amino acids, containing between 3 and 7 carbon atoms. The lactams include γ-butyrolactam, δ-valerolactam and ε-caprolactam. The reaction of these lactams with an alkali metal is believed to proceed as set forth in the following equation: ##STR3## wherein R¹ and M are as previously defined.

The hexaorgano distannanes that prevent or inhibit discoloration of the foregoing lactam derivatives exhibit the general formula R₃ ² Sn--SnR₃ ³ wherein R² and R³ each represent an alkyl radical which may contain between 1 and 20 carbon atoms, a cycloalkyl, aralkyl, alkaryl or an aryl radical. Suitable alkyl radicals include methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl and higher homologs containing between 5 and 20 carbon atoms. Alternatively, one of the hydrogen atoms of the alkyl radical can be replaced by an aryl radical, yielding an aralkyl radical such as benzyl or β-phenylethyl. Cycloalkyl radicals include cyclopentyl, cyclohexyl and cyclooctyl. Aryl radicals which can be represented by R² and/or R³ include phenyl and naphthyl. One or more hydrogen atoms of the aryl radical can be replaced by a methyl or other alkyl radical to form an aralkyl radical such as o-, m- or p-tolyl or one of the isomeric xylyl radicals. Preferably R² and R³ represent alkyl radicals containing between 1 and 4 carbon atoms. It should be pointed out that while R² and R³ are preferably identical, this is not a requirement. Methods for preparing "unsymmetrical" hexaorgano distannanes are well known in the art, for example by the reactions described by W. P. Neumann et al. [Annalen der Chemie, Vol. 692, pages 1-11 (1966)].

The minimum concentration of organotin compound required to prevent or inhibit discoloration of compositions containing the alkali metal salt of a lactam depends to a large extend upon the length of time during which the composition will be stored and the temperatures to which the mixture will be exposed during processing and storage. A concentration of between 0.5 and 100%, based on the weight of alkali metal salt, is usually sufficient to prevent or at least significantly reduce the discoloration which occurs during formation and storage of the salt. As will be described in the examples which form part of this specification, the salts are often prepared by addition of the alkali metal to the molten lactam under an inert atmosphere such as nitrogen. The preferred lactam, ε-caprolactam, is a solid that melts at 69° C. The amount of alkali metal added can be sufficient to react with all of the lactam present in the reaction mixture. If the resultant salt is to be employed as the catalyst for a lactam polymerization, it is common practice to employ only enough alkali metal to yield the concentration of salt required to catalyze the polymerization. The amount of catalyst usually is between 0.05 and 5%, based on the weight of lactam. Alternatively, a mixture of lactam and the alkali metal salt thereof can be employed as a catalyst concentrate which is subsequently combined with additional lactam prior to polymerization to achieve the desired catalyst concentration. The mixture of salt and lactam is then heated under an inert atmosphere at temperatures between 200° and 300° C. for a length of time sufficient to achieve the desired molecular weight.

The present alkali metal salts of lactams can be employed as catalysts for the copolymerization of two or more lactams or a polymerization involving one or more lactams and one or more lactones. The lactams preferably contain 5 or 7 atoms in the ring whereas the lactones contain 4, 6 or 8 atoms.

The following examples demonstrate preferred embodiments and should not be interpreted as limiting the scope of the invention defined in the appended claims.

EXAMPLE 1

The compositions employed to evaluate the stabilizers were prepared by transferring 50 cc. samples of molten ε-caprolactam under a nitrogen atmosphere into containers which had previously been filled with nitrogen and charged with the desired amount of stabilizer. The containers were then placed in a water bath maintained at a temperature of 73° ± 2° C. Between 0.18 and 0.20 g. of sodium metal was then placed in each of the containers. The resultant hydrogen evolution was allowed to continue for between 3 and 5 minutes, as required, at which time the containers were sealed and the temperature of the water bath raised to 80° ± 5° C. The samples remained in the water bath for 24 hours, at which time they were removed and allowed to cool. The yellowness index of the resultant solid materials were measured using a Meeco Colormaster Differential Colorimeter manufactured by Manufacturers Engineering and Equipment Corp. This instrument measures the percent green, red and blue light which is reflected from the sample. The yellowness index (Y.I.) is calculated using the equation Y.I. =(% red reflectance - % blue reflectance) /% green reflectance.

Since the discoloration of the sodium salt in almost all instances produces a shade of yellow, the yellowness index provides a suitable means for determining the stability imparted by the various compounds tested. By definition the yellowness index is directly proportional to the intensity of this color.

The yellowness index values obtained using a variety of known stabilizers, including the present hexaorgano distannanes are recorded in the following table together with the amount of stabilizer present in the test sample.

    ______________________________________                                         Stabilizer    Amount (g.) Yellowness Index                                     ______________________________________                                         None (control)                                                                               --          0.385, 0.385 (2 trials)                              hexamethyl distannane                                                                        0.2         0.160                                                hexamethyl distannane                                                                        0.1         0.166                                                hexabutyl distannane                                                                         0.2         0.193                                                hexabutyl distannane                                                                         0.1         0.243                                                Controls (prior art stabilizers)                                               butyl stannoic acid                                                                          0.2         0.300                                                2,4-di-t-butyl-p-cresol                                                                      0.2         0.304                                                di-n-butyltin-S,S'-bis                                                         (lauryl mercaptide)                                                                          0.2         0.308                                                bis(tri-n-butyltin)                                                            oxide         0.2         0.335                                                tetrabutyltin 0.2         0.359                                                stannous oxalate                                                                             0.2         0.373                                                triphenyl phosphine                                                                          0.2         0.384                                                triphenyl antimony                                                                           0.2         0.466                                                ______________________________________                                    

The foregoing data demonstrate that the intensity of the yellow color which develops in compositions containing the sodium salt of ε-caprolactam and the present hexaorgano distannanes is considerably less when compared against identical compositions containing known organotin and other stabilizers, even those which the prior art discloses as being effective stabilizers for polyamides. For example, U.S. Pat. No. 3,189,575 discloses that various classes of organotin compounds, including tetraorganotin compounds, organotin halides, -oxides, -sulfides and compounds containing bonds from tin to nitrogen or phosphorus are useful stabilizers for polyamides.

EXAMPLE 2

A polymer of ε-caprolactam was prepared by adding 0.2 g. of sodium metal and 0.2 g. of hexabutyl distannane to a 50 cc. sample of ε-caprolactam under the conditions described in Example 1. The sample was then heat treated at 80° ± 5° C. for 24 hours. The sealed container was then placed inside a steel pipe. The pipe was sealed on both ends and then placed in a circulating air oven heated to a temperature of 250° C. for 1 hour. The resultant polymer was off-white in color and exhibited an inherent viscosity of 0.79 measured at 25° C using a solution containing 0.5% of polymer in meta-cresol. This corresponds to a number average molecular weight of 11,000.

A mixture of ε-caprolactam and the sodium salt thereof which did not contain any stabilizer was prepared and polymerized as described in the preceding paragraph. The polymer exhibited an inherent viscosity of 0.54, which corresponds to a number average molecular weight of 6200.

The number average molecular weight for each of the foregoing polymer samples was calculated using the formula

    M.sub.n = 15,600 ×(η.sub.inh) .sup.1.49 .

M_(n) represents the number average molecular weight and η_(inh) the inherent viscosity. 

What is claimed is:
 1. In a fiber-and film-forming lactam polymer composition which contains between 0.05 and 5%, based on the weight of said polymer, of an alkali metal salt of said lactam, the improvement which resides in the presence in said composition of between 0.5 and 100%, based on the weight of said alkali metal salt, of a hexaorgano distannane exhibiting the formula R₃ ² SnSnR₃ ³, wherein R² and R³ are each selected from the group consisting of alkyl radicals containing between 1 and 20 carbon atoms.
 2. The lactam polymer composition of claim 1 wherein R² and R³ are butyl radicals.
 3. The lactam polymer composition of claim 1 wherein the lactam is ε-caprolactam.
 4. The lactam polymer composition of claim 1 wherein the alkali metal is sodium. 